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1984 1
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Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.
Roomans GM, Ivanovs A, Shebani EB, Johannesson M. Roomans GM, et al. Ups J Med Sci. 2006;111(1):155-68. doi: 10.3109/2000-1967-010. Ups J Med Sci. 2006. PMID: 16553254 Review.
Primary ciliary dyskinesia (PCD) is an autosomal recessive disease with extensive genetic heterogeneity. Dyskinetic or completely absent motility of cilia predisposes to recurrent pulmonary and upper respiratory tract infections resulting in bronchiectasis. ...The best met …
Primary ciliary dyskinesia (PCD) is an autosomal recessive disease with extensive genetic heterogeneity. Dyskinetic or completely absent
[How useful is the ultrastructural study of the cilia of the respiratory tract in the diagnosis of an immotile cilia syndrome?].
Fischer L, Burri PH, Bauer W, Kraemer R, Sauter K. Fischer L, et al. Schweiz Med Wochenschr. 1984 May 5;114(18):610-9. Schweiz Med Wochenschr. 1984. PMID: 6374886 Review. German.
In no instance did a patient show only a single anomaly; defects were always combined. Missing dynein arms, radial spoke defects and microtubular transpositions have frequently been described as lesions specific for ICS. Whenever these lesions were found simultaneou …
In no instance did a patient show only a single anomaly; defects were always combined. Missing dynein arms, radial spoke defec …